US20080257359A1 - Apparatus And Related Method For Providing A Passage Into The Body - Google Patents
Apparatus And Related Method For Providing A Passage Into The Body Download PDFInfo
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- US20080257359A1 US20080257359A1 US12/043,849 US4384908A US2008257359A1 US 20080257359 A1 US20080257359 A1 US 20080257359A1 US 4384908 A US4384908 A US 4384908A US 2008257359 A1 US2008257359 A1 US 2008257359A1
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- Prior art keywords
- slider
- scalpel
- slider unit
- tissue spreader
- tissue
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- GNOGWEUBBIRUSL-UHFFFAOYSA-N CC(C)CC1(C)C=C(C2)C2C1 Chemical compound CC(C)CC1(C)C=C(C2)C2C1 GNOGWEUBBIRUSL-UHFFFAOYSA-N 0.000 description 1
- GDOPTJXRTPNYNR-UHFFFAOYSA-N CC1CCCC1 Chemical compound CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 1
- GLMBMTQCXYBJRS-VURMDHGXSA-N CCCC(C)(CC(C)CC1/C=C\C)C1=C Chemical compound CCCC(C)(CC(C)CC1/C=C\C)C1=C GLMBMTQCXYBJRS-VURMDHGXSA-N 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
- A61M16/04—Tracheal tubes
- A61M16/0465—Tracheostomy tubes; Devices for performing a tracheostomy; Accessories therefor, e.g. masks, filters
- A61M16/0472—Devices for performing a tracheostomy
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/32—Surgical cutting instruments
- A61B17/3209—Incision instruments
- A61B17/32093—Incision instruments for skin incisions
Definitions
- the disclosure relates generally to a surgical instrument such as an apparatus and method for providing a passage into the body, and more particularly, the disclosure relates to a percutaneous or a non-dissection apparatus and method for use in, among other things, establishing an airway in medical procedures including tracheostomies and cricothyroidectomies.
- a first responder In certain patient care situations, a first responder must immediately establish and maintain a patient's airway. Once an airway is established, the first responder must determine whether the patient is breathing. If breathing is adequate, maintenance of the airway should be continued. If breathing is inadequate, or absent, artificial respiration should be initiated.
- a tracheotomy is generally defined as a temporary or permanent treatment for a variety of causes of breathing difficulties in which the creation of a new breathing pathway is required to by-pass the nose, mouth, and upper throat.
- a tracheotomy is usually considered when an endotracheal (ET) tube (a tube that goes in the throat through the mouth) will not be effective (in some emergency situations for example), or would be required for a long time.
- ET endotracheal
- a tracheotomy is performed when an ET tube cannot be placed due to narrowing of the windpipe, blockage of the voice box (larynx) or facial trauma prevents intubation via the ET tube.
- a cricothyrotomy (also called thyrocricotomy, cricothyroidotomy, inferior laryngotomy, intercricothyrotomy, coniotomy or emergency airway puncture) is an emergency incision through the skin and cricothyroid membrane to secure a patient's airway for emergency relief of upper airway obstruction.
- a cricothyrotomy is usually performed by paramedics and emergency physicians as a last resort in cases of severe choking due to upper airway obstruction when attempts at orotracheal and nasotracheal intubation have failed.
- percutaneous or non-dissection devices and techniques are normally preferably to dissection procedures, which require considerable more surgical skills in that many blood vessels are involved which tend to bleed profusely during a dissection procedure.
- combat casualty care that is, providing cricothyroidectomies in a field environment
- Performing successful cricothyroidectomies has been identified as one of the three most important procedures for saving soldier's lives.
- Field cricothyroidectomies are critical to maintain life and provide severely injured far-forward battlefield participants an opportunity to survive until treated in a battlefield treatment facility.
- the current overall complication rate of a combat cricothyrotomy is 32% or 5 times higher than the complication rate when the procedure is conducted under controlled circumstances.
- Duress, adverse conditions, and non-standardization of airway kits all contribute to a high complication rate, including errors in incision location and incision depth in “combat care situations”.
- a currently available airway device includes the Rusch QuickTrach sold by a number of on-line distributors.
- Other airway devices include those described in U.S. Pat. No. 4,520,810 issued Jun. 4, 1985 to Weiss; U.S. Pat. No. 4,677,978 issued Jul. 7, 1987 to Melker; U.S. Pat. No. 4,978,334 issued Dec. 18, 1990 to Toye et al.; and U.S. Pat. No. 5,217,005 issued Jun. 8, 1993 to Weinstein, and the common #11 surgical scalpel and well-known endotracheal breathing tube.
- the subject matter described herein relates generally to a surgical instrument such as an apparatus and method for providing a passage into the body and displacement (spreading) of incised tissue, and more particularly, to a percutaneous or a non-dissection apparatus and method having universal and common components and methodology of execution for use in, among other things, establishing an airway in medical procedures including tracheostomies and cricothyroidectomies.
- the device described herein for providing a passage into the body includes, a housing, and a scalpel and a tissue spreader disposed within the housing along a common slider track for extension and retraction (deployment) of the scalpel and the tissue spreader from the same side of the housing.
- the tissue spreader includes a bifurcated leading edge formed by a first arm and a second arm, and configured to move from a closed position to an open position upon retractable deployment of the tissue spreader to open a site of incision for acceptance of a breathing tube.
- an apparatus for providing a passage into the body comprises a housing; a slider track formed within the housing; and a first slider unit configured to retain a scalpel and a second slider unit configured to retain a tissue spreader each operably connected to the slider track for movement along the slider track.
- an apparatus for providing a passage into the body includes a first slider unit and a second slider unit operably connected to a slider track for retractable deployment of a scalpel and a tissue spreader attached respectively thereto, and for the auto-retraction of the scalpel due to movement of the second slider unit.
- the device described herein for establishing an airway provides, among other things, (1) visible and infra-red light sources, (2) a combination of a clean retractable scalpel and a tissue spreader device, (3) incision depth gauging and regulation, (4) tissue preparation and administration components, (5) an endotracheal tube, and (6) a tube stabilization device all integrated into a durable, compact, lightweight, ergonomic hand-held device for one-hand operation (7) integrated tissue “hook” (commonly known and referred to as a “trach hook” for additional means of displacing incised tissue.
- integrated tissue “hook” commonly known and referred to as a “trach hook” for additional means of displacing incised tissue.
- FIG. 1A shows one embodiment of a durable, compact, lightweight, ergonomic hand-held device having universal and common components and methodology of execution for use in, among other things, one-hand operation in providing an opening into the body such as in establishing an airway in medical procedures including tracheostomies and cricothyroidectomies.
- FIGS. 1B-1C show cutaway views of the apparatus shown in FIG. 1A .
- FIGS. 2A-2F illustrate one method of performing or executing an emergency tracheotomy (cricothyroidectomy) utilizing the device described herein.
- FIG. 3 shows tracheal and associated tissue depths for selected persons, and proposed scalpel depth information for retractable deployment of the scalpel.
- FIGS. 4A-4E show various views of the device shown in FIG. 1A , and more particularly, show the same-side retractable deployment relationship of a scalpel and a tissue spreader along a common slider track in accordance with one embodiment ( FIG. 4E ), and an opposite side retractable deployment relationship of a scalpel and a tissue spreader along a common slider track in accordance with another embodiment ( FIG. 4D ).
- FIGS. 5A-5B show movement of the slider switch and corresponding tissue spreader switch along the slider track to an extension depth of 10 mm.
- FIGS. 6A-6B are similar to FIGS. 5A-5B and show movement of the slider switch and corresponding tissue spreader switch along the slider track to an extension depth of 15 mm.
- FIGS. 7A-7B show movement of the slider switch and corresponding tissue spreader switch along the slider track to an extension depth of 20 mm.
- FIGS. 8A-8E show top, side, side with “Quick Trach” cartridge inserted and withdrawn from a housing, back, and front views, respectively of an alternative embodiment of a device in accordance with an embodiment.
- FIGS. 9A-9L show various views of one embodiment having a removably attached combination tracheal “hook” and tissue-spreader tool.
- FIGS. 10A and 10B shows a general-purpose tool for providing a passage into the body in accordance with one embodiment.
- FIG. 11A is top view of the tool of the tool shown in FIGS. 10A and 10B showing a scalpel extended between an elongated slit formed in the “hooked” protrusion.
- FIG. 11B and FIG. 11C respectively show side views of the tool with the scalpel in an extended and retracted position.
- FIG. 11D shows a front view of the tool including a first extension and a second extension of a bifurcated end, the “hooked” protrusion with its elongated slit, and the scalpel.
- FIG. 11E shows a side view of the tool with the sides of the tool body removed to show the connection between the slider switch and the scalpel.
- FIG. 11F shows the bifurcated end of the tool and illustrates a general range of motion of the tissue spreader.
- FIGS. 12A-12E show an apparatus for providing a passage into the body in accordance with another embodiment.
- FIGS. 13A-13C and FIGS. 14A-14D show an apparatus for providing a passage into the body in accordance with still another embodiment.
- FIGS. 15A-15E show an apparatus for providing a passage into the body in accordance with still another embodiment.
- FIGS. 16-19 and 20 A- 20 D show an apparatus for providing a passage into the body in accordance with still another embodiment.
- tracheotomy and cricothyroidotomy are considered to be interchangeable for purposes of explaining the subject matter provided herein.
- the device described herein provides for a compact universal cricothyrotomy (CRIC) kit that is relatively safer, more efficient, consistent, and easier to use when executing or providing an opening into the body, such as when performing an emergency tracheotomy, in all environments, including dark and “hot” combat theater situations, when compared to known emergency tracheotomy devices.
- CRIC compact universal cricothyrotomy
- the device provides, among other things, (1) visible and infra-red light sources, (2) a combination of a clean retractable scalpel and a tissue spreader device, (3) incision depth gauging and regulation, (4) tissue preparation and administration components, (5) a standard (6 mm) endotracheal tube, and (6) tube stabilization device all integrated into a durable, compact, lightweight, ergonomic hand-held device for one-hand operation in establishing an airway.
- FIG. 1A shows a side view of one embodiment of the device or CRIC kit 5 .
- this embodiment of the device 5 includes a curved ergonomically shaped housing 10 designed to fit in the palm of a person's hand.
- the housing 10 is constructed from molded plastic such as a polycarbonate, polypropylene, etc.
- molded plastic such as a polycarbonate, polypropylene, etc.
- other plastics, as well as other materials such as metals, composites, glass, rubber, and the like, in the construction of the device will depend on a number of factors including, for example, material cost, durability, and the intended use of a part.
- the housing 10 includes a flip tab 15 positioned to rotatably open a storage hatch 20 about a rotatable hinge 25 for accessing a storage compartment 30 for retention of tissue preparation components such as prep-wipes 40 , retainer strap 35 for endotracheal tube stabilization, and access to a standard 6 mm endotracheal breathing tube 45 (see also FIGS. 2A-2F ) that are positioned within a tube cavity 50 formed within the housing 10 .
- tissue preparation components such as prep-wipes 40
- retainer strap 35 for endotracheal tube stabilization
- a standard 6 mm endotracheal breathing tube 45 see also FIGS. 2A-2F
- cuff retainers 55 ( a ), 55 ( b ) having retainer strap slits 56 ( a ), 56 ( b ) positioned on opposite sides of the enodtracheal tube 45 are available to assist the user in removing the endotracheal tube 45 from the tube cavity 50 .
- the cuff retainers 55 ( a ), 55 ( b ) extend outside of the housing 10 .
- the housing 20 further includes a first slider switch 60 for extending and retracting a scalpel 65 ( FIG. 2C ), and a second slider switch 70 for extending and retracting a tissue spreader 75 .
- the scalpel 65 and tissue spreader 75 are operably connected to respective slider switches 60 , 70 by well-known means such as those methods used to extend and retract the blade of a box cutter.
- the scalpel 65 and tissue spreader 75 are disposed or stored safely and conveniently within housing 10 .
- the first slider switch 60 and second slider switch 70 are positioned within a slider track 80 for extending and retracting the scalpel 65 and tissue spreader 75 away from the housing 10 and toward the housing 10 .
- the device described herein provides for retractable deployment of a scalpel 65 and a tissue spreader 75 along a common slider track 80 .
- the first or scalpel slider switch 60 is positioned forward of the second or tissue spreader slider switch 70 within the slider track 80 for retractable deployment from the same side of the device 5 .
- the first or scalpel slider switch 60 is positioned to retractably deploy from one end of the device 5 while the second or tissue spreader slider switch 70 is positioned to retractably deploy from the opposite end of the device 5 .
- a single slider track 80 or dual slider tracks may be utilized for retractable deployment of the first switch 60 and second switch 70 .
- the slider track 80 may include a plurality of detents 85 ( a )-( c ) positioned at prescribed intervals to provide incision-deep regulation, gauging, and feedback to the user as to the extended or retracted distance of the scalpel 65 (see FIG. 5A ).
- Scalpel distance demarcations 90 ( a )-( c ) may also be provided for incision-depth regulation and gauging by visual verification and confirmation of the scalpel 65 extension or retraction distance. In one example, verification of scalpel distance positioning is provided by markings such as 10, 15, and 20 millimeters molded directly into the housing 10 . These markings 90 ( a )-( c ) confirm the scalpel positioning as provided by the detents 85 ( a )-( c ) on the associated slider track 80 .
- the scalpel switch 60 is moved from left to right in each of the figures from a first detent position 85 ( a ) to a second and a third detent position 85 ( b ), 85 ( c ), the scalpel 65 is moved outward from the housing 10 approximately 10 mm, 15 mm, and 20 mm.
- the housing 10 also provides for switch and/or pushbutton 95 , 96 activation and verification of IR (infrared) and visible light spectrum LEDs 100 , 105 mounted on the front-underside of the housing 10 .
- Lithium ion batteries 110 are housed within the housing 10 to provide power to the LEDs 100 , 105 .
- “Gripper nubs” (raised bumps) 115 may be molded into the housing 10 or formed from rubber and applied to the housing 10 to provide a textured surface to assist the user in holding, gripping, or otherwise maneuvering the device 5 .
- the device 5 is a relatively simple, safe, and easy to use device.
- use of the device 5 to establish an airway in medical procedures begins by opening the storage hatch 20 , removing one or more prep-wipes/pads 40 , and wiping the intended site or area of incision 120 for establishment of an airway.
- the storage hatch 20 is closed and depending on the lighting conditions either the IR LED light 100 or visible-spectrum LED light 105 may be activated by the associated single pushbutton membrane or switch 95 , 96 to illuminate the site of incision 120 .
- FIG. 1 the IR LED light 100 or visible-spectrum LED light 105 may be activated by the associated single pushbutton membrane or switch 95 , 96 to illuminate the site of incision 120 .
- establishing an airway then proceeds by deploying or extending the scalpel 65 a predetermined distance (10 mm, 15 mm, or 20 mm) as indicated by the scalpel demarcations 90 ( a )-( c ) and/or the detents 85 ( a )-( c ).
- the device 5 provides for safe extension and retraction (deployment) of the scalpel 65 by a half-circle slider switch 60 moved along a slider track 80 having detents 85 ( a )-( c ) position to indicate the scalpel 65 extension and retraction distances of 10 mm, 15 mm, and 20 mm from the housing 10 , as well as the extension and retraction of an associated tissue spreader 70 by a corresponding half-circle slider switch 70 .
- the 10, 15, and 20 millimeter depth of the scalpel 65 is generally shown as approximating the centerline depth of the trachea for 50% of certain individuals.
- persons 6-8 years old generally require an incision depth of 10 mm, soldiers a depth of 15 mm, and overweight adults a depth of 20 mm.
- extension of the scalpel 65 to the appropriate depth ensures adequate penetration through the outer skin (epidermis), cricocartilage, and anterior wall of the trachea, while preventing too-deep penetration of the scalpel 65 that could potentially cause damage to the posterior tracheal inner surface.
- the front of the housing 125 acts as a buffer or barrier to prevent further movement of the scalpel 65 into the trachea cavity that may result in excessive penetration of the scalpel 65 beyond the selected penetration/extension depth 85 ( a )-( c ), which results in damage to the trachea wall and/or other vital areas such as the esophagus.
- scalpel depths may replace and/or supplement those indicated above.
- the tissue spreader 75 is extended forward along the slider track 80 using a half-circle slider switch 70 similar to the half-circle slider switch 60 used to extend the scalpel 65 forward.
- the half-circle tissue spreader slider switch 70 is brought forward to mate with the half-circle scalpel slider switch 60 .
- Mating of the tissue spreader switch 75 with the scalpel switch 60 is further shown in FIGS. 5B , 6 B, and 7 B at 10 mm, 15 mm, and 20 mm, respectively along the slider track 80 .
- Movement of the tissue spreader slider switch 70 along the slider track 80 until it mates with the scalpel slider switch 60 permits a bifurcated tapered leading end 130 of the tissue spreader 75 to: (1) slide forward in a “closed” position “hugging” the scalpel 65 , (2) to eventually penetrate into the tracheal cavity through the incision created by the scalpel 65 , and (3) to move from the “closed” position to an “open” position to spread the incision to an approximate distance of 1.27 centimeter (0.5′′) to allow room for insertion of the breathing tube 45 .
- the device 5 may be designed so that the tissue spreading distance may vary from the distance stated above to accommodate other size tubes or similar articles for maintaining an airway.
- opening or spreading of the scalpel's bifurcated leading edge 130 is facilitated by the enlarged distal end 135 (i.e., that end of scalpel opposite the cutting end 140 ) of the scalpel 65 positioned between a first arm 140 and a second arm 141 of the tissue spreader 75 .
- the enlarged distal end 135 of scalpel 75 forces the tapered trailing end 145 of the tissue spreader 75 apart, resulting in a similar spreading apart of the leading end 130 of the tissue spreader 75 .
- Mating of the tissue spreader switch 70 with the scalpel switch 60 acts to regulate and correspond the depth of tissue spreader 75 penetration into the incision opening with the depth of scalpel 65 penetration into the incision opening.
- retractable deployment distance of the tissue spreader is such that the tissue spreader 75 extends beyond the retractable deployment distance of scalpel 65 to permit insertion of the endotracheal breathing tube 45 into the incision site without removal of the tissue spreader 75 from the incision.
- the endotracheal tube 45 and endotracheal tube retainer or tie-down strap 35 are removed from the storage compartment 30 .
- the endotracheal tube 45 is then inserted between the bifurcated leading end 130 of the tissue spreader 75 and into the incision opening.
- the device 5 (including the tissue spreader 75 ) is retracted or removed from the incision, and the endotracheal tube retainer strap 35 is attached to endotracheal tube 45 along the cuff retainer slits 56 ( a )-( b ) and tied around the patient's neck to secure the endotracheal tube 45 in place.
- the device 145 includes a reusable housing 150 with a butterfly-opening latch 147 , and a slidable cartridge housing 146 that moves and deploys the inserted disposable/replaceable pro-trach cartridge 155 temporarily retained therein for storage and deployment in establishing an airway.
- the cartridge 155 includes a combination piercing tube 156 surrounding by a sleeve 157 .
- a storage compartment 160 is provided to retain an industry standard 12 mm breathing tube adaptor 170 .
- the breathing tube adapter 170 is attached to the sleeve 157 to maintain establishment of the airway. Accordingly, one method of establishing an airway using the device shown in FIGS.
- 8A-8E includes, bringing the piercing tube 156 and associated sleeve 157 forward by slide switch 158 , 159 activation to the site of intended incision, making an incision using the piercing tube 156 , and inserting the sleeve 157 into the site of incision by the continued forward movement of the combination piercing tube 156 and sleeve 157 .
- the sleeve 157 and piercing tube 156 are released from the housing 150 by the butterfly latch 147 to remain disposed within the incision site.
- the housing 150 is made available for accepting another similarly constructed pro-trach cartridge 155 therein for use in establishing an airway.
- the 12 mm breathing tube adaptor 170 is then removed from the storage compartment 160 , attached to the sleeve 157 by threading, friction fit, or a similar attachment means, and retained in place to maintain establishment of the airway.
- the device 5 may further include a removably attached combination tracheal “hook” and tissue-spreader tool 200 .
- the combination tool 200 is of a general durable, sterilizable, single-piece injection molded, translucent polycarbonate material construction. Although the length of the combination tool 200 may vary, a combination tool 200 length of approximately 4.5 inches is typically adequate for most applications.
- the shape of combination tool 200 corresponds to the shape of the housing 10 so that when placed in a closed or retracted position (explained below) the tool 200 stores directly onto the CRIC housing 10 .
- the combination tool 200 includes a first end 201 having a “hook” shaped tip 202 , and a bifurcated second end 203 (opposite the first end 201 ) having a first leg 204 A and a second leg 204 B biased in a normally open position.
- the combination tool 200 further includes a first extension 205 A positioned on one leg 204 A of the bifurcated end 203 , and a second extension 205 B positioned on the other leg 204 B of the bifurcated end 203 .
- the shape of the first extension 205 A and second extension 205 B may vary to facilitate compression or closing of the bifurcated second end 203 .
- a dual-purpose a first stem 206 A is positioned at the tip of one leg 204 A and a dual-purpose second stem 206 B is positioned at the tip of the other leg 204 B.
- Each extension 205 A, 205 B, and each stem 206 A, 206 B extend laterally from the combination tool 200 .
- the shape of the first stem 206 A and second stem 206 B may likewise vary to facilitate the necessary spreading of tissue as intended by the bifurcated second end 203 .
- the opening between the legs 204 A, 204 B of the bifurcated end 203 of the combination tool 200 in a relaxed state shown in FIG.
- the opening between the legs 204 , 204 B of the bifurcated end 203 of the combination tool 200 in a compressed state is approximately 0.13 inches.
- protrusions 210 A, 210 B having locating holes positioned 211 A, 211 B therein are molded into the housing 10 of the device 5 for removably receiving an associated stem 206 A, 206 B so as to rotatably retain the combination tool 200 onto the housing 10 .
- force applied in the direction of arrows “A” ( FIG. 9C ) to the first and second extensions 205 A, 205 B typically by squeezing or flexing the extensions toward each other, brings together the first and second stems 206 A, 206 B.
- the stems 206 A, 206 B are then positioned between the protrusions 210 A, 210 B so that the stems 206 A, 206 B lineup with the locating holes 211 A, 211 B.
- Force applied to the first and second extensions 205 A, 205 B is then removed causing the bifurcated second end 203 to move in the direction of arrow “B” ( FIG. 9C ), biasing the second end 203 to the open position, and permitting the stems 206 A, 206 B to be removably received into the locating holes 211 A, 211 B.
- the combination tool 200 is capable of being rotated approximately 180 degrees from a closed or retracted position ( FIG. 9A ) to an open or extended position ( FIG. 9B ).
- a retaining clip 215 having detents (not shown) formed therein is molded into the housing 10 to further assist in retaining the combination tool 200 by holding, gripping, or otherwise securing the first end 201 of combination tool 200 while in the closed position.
- the housing 10 is molded to include a “sheath” like storage extension 220 for protecting the “hook” shaped tool 202 during storage of the combination tool 200 .
- the “sheath” like extension 220 may be constructed to include the retaining clip 215 mention above, or a trough of reduced width may be included to frictionally secure the first end 201 of the combination tool 200 .
- the combination device 200 may remain attached to the housing 10 and rotated into the extended position so that the “hook” shaped tip 202 of the first end 201 may be inserted into a previously made incision in the tissue.
- the tissue may then be distended by moving the device 5 with attached “hook” in direction “C” ( FIG. 9C ) so the incision and/or tissue may be irrigated, for example.
- the combination device 200 may be removed from the housing 10 and used independently as a stand alone tool or in conjunction with the various design features of the device 5 explained above.
- the lateral stems 206 A, 206 B of the bifurcated second end 203 previously used to rotatably retain the combination device 200 to the housing 10 , are made available for insertion into an incision.
- the bifurcated second end 203 spreads the tissue apart a minimum of 6 mm to accommodate a standard size endotracheal tube 45 or similar device.
- Variations of the combination tool shown in at least FIGS. 9C and 9F include modifications to the length and shape of the space or opening 230 extending between the opposite legs 204 A, 204 B of the bifurcated end 203 to facilitate spreading of the legs or tines 204 A, 204 B, as well as the addition of integrated thumb/finger recesses 235 A, 235 B along the sides of the combination tool 200 .
- the device may be embodied in the form of a general-purpose tool 300 for providing a passage into the body.
- the tool 300 includes a tool body 305 , preferably of a one-piece molded construction, having an elongated slider track 310 formed therein.
- the tool 300 preferably further includes a slider switch 315 movably disposed within the slider track 310 for extending and retracting a scalpel 320 from a first side 325 of the tool body 305 .
- the scalpel 320 In the retracted position the scalpel 320 is housed between opposite sides 345 , 350 of the tool body 305 .
- the tool body 305 may be “safely” handled, carried, or otherwise manipulated as the scalpel 320 is stored within the tool body 305 .
- the tool body 305 may be constructed of a semi-translucent material, such as plastic, to provide visual assessment of the scalpel 320 position as well as the tissue area of the patient.
- the tool body 305 further includes a “hook” shaped protrusion 321 extending from the same side 325 of the tool body 305 as the scalpel 320 when the scalpel 320 is in an extended position.
- the extension 321 includes an elongated slit 322 ( FIG. 10B ) generally located in the center of the “hooked” protrusion 321 for receiving the scalpel 320 therethrough when the scalpel 320 is extended from the tool body 305 .
- the protrusion 321 functions as a depth guard for the scalpel 320 when making a tissue incision, and as a “hook” 321 for tissue displacement when the scalpel 320 is retracted.
- typical scalpel 320 extension from the protrusion 321 is generally limited to less than 16 mm.
- a tissue spreader 330 having a bifurcated end 335 may be included and located on a second or opposite side 340 of the tool body 305 .
- the bifurcated end 335 includes a first leg 360 A and a second leg 360 B biased in an open position.
- the tool 300 further includes a first extension 365 A positioned on one leg 360 A of the bifurcated end 335 , and a second extension 365 B positioned on the other leg 360 B of the bifurcated end 335 .
- the tool 300 shown in FIG. 10A and FIG. 10B at least with respect to the “hook” shaped protrusion 321 and the bifurcated tissue spreader 330 is substantially similar to use of the combination tool 200 shown in FIGS. 9A-9D above.
- the tool 300 shown in at least FIGS. 10A and 10B further includes a retractable scalpel 320
- the tool 300 may generally be considered an all or multi-purpose tool for providing a passage into the body.
- FIGS. 11A-11G show various views of the multi-purpose tool 300 described above.
- FIG. 11A is top view of the tool 300 showing the scalpel 320 extended between the elongated slit 322 formed in the “hooked” protrusion 321 .
- Side views of the tool 300 with the scalpel 320 in an extended and a retracted position are shown in FIG. 11B and FIG. 11C , respectively.
- FIG. 11D shows a front view of the tool 300 including the first extension 365 A and a second extension 365 B of the bifurcated end 335 , the “hooked” protrusion 321 with its elongated slit 322 , and the scalpel 320 .
- FIG. 11A is top view of the tool 300 showing the scalpel 320 extended between the elongated slit 322 formed in the “hooked” protrusion 321 .
- Side views of the tool 300 with the scalpel 320 in an extended and a retracted position
- FIG. 11E is a side view of the tool 300 with the sides 345 , 350 of the tool body 305 removed to show the connection between the slider switch 315 and the scalpel 320 .
- FIG. 11F shows the bifurcated end 335 of the tool 300 and illustrates a general range of motion of the tissue spreader 330 .
- FIGS. 12A-12E A further embodiment of a general-purpose tool 400 for providing a passage into the body is shown in FIGS. 12A-12E .
- many of the design features found in the multi-purpose tool 300 shown in at least FIG. 10A and FIG. 10B including a tool body 405 , a slider track 410 formed therein, and a slider switch 415 disposed within the slider track 410 for extending and retracting a scalpel 420 from a first side 425 of the tool body 405 .
- this embodiment of the tool 400 includes a depth guard/“hook”/tissue spreader combination 430 integrated into a single device on the same side 425 of the tool body 405 as the scalpel 420 when extended from the tool body 405 .
- the integrated device 430 combines a tissue “hook” 435 , incision depth guard 440 (provided by the front face of the tissue hook 435 , tissue hook 440 ), and tissue spreader 445 having a bifurcated end 450 .
- the bifurcated end 450 includes a first leg 460 A and a second leg 460 B generally biased in a closed position ( FIG. 12A ), and a first rotatable arm 465 A connected to the first leg 460 A and second rotatable arm 465 B connected to the second leg 460 B for rotatably positioning the first and second legs 460 A, 460 B of the tissue spreader 445 in an open position.
- activation of the tissue spreader device of FIG. 12B is provided by the rotatable arms 465 A, 465 B connected to a corresponding tissue spreader leg 460 A, 460 B and rotating along rotation paths designated as “R 1 ” and “R 2 ” in FIG. 12B .
- rotation of each rotatable arm 465 A, 465 B toward the tool body 405 opens or spreads the first leg 460 A and second leg 460 B of the bifurcated end 450 while rotation of each rotatable arm 465 A, 465 B away from the tool body 405 closes or brings together the first leg 460 A and the second leg 460 B of the bifurcated end 450 .
- the combination device 430 allows the scalpel 420 to pass between the legs 460 A, 460 B of the tissue spreader 445 to permit an incision to be made in a patient ( FIG. 12D and FIG. 12E ).
- the incision depth guard 440 maintains a scalpel 420 incision depth of less than 16 mm.
- 5A-7B may be provided on the tool body 405 thereby providing for variable extension depths of the scalpel 420 and/or opening distances of the tissue spreader 445 .
- the maximum distance between the open legs 460 A, 460 B of the tissue spreader is 19 mm.
- any distance/measurement discussed within the detailed description regardless of whether the distance/measurement refers to some aspect of the scalpel, tissue spreader, or hook, is not meant to be an absolute distance/measurement in that the distance/measurement may vary depending on any number of factors, including the device's intended use.
- the device 500 includes including a housing 505 , a slider track 510 formed therein, and a slider switch 515 disposed within the slider track 510 for extending and retracting a scalpel 520 from a first side 525 of the housing 505 .
- the housing 500 shown in FIGS. 13A-13C further includes a bifurcated depth guard/“hook”/tissue spreader combination 530 integrated into a single device on the same side 525 of the housing 505 as the scalpel 520 when extended from the tool body 505 .
- a bifurcated depth guard/“hook”/tissue spreader combination 530 integrated into a single device on the same side 525 of the housing 505 as the scalpel 520 when extended from the tool body 505 .
- tissue depth guard/“hook”/tissue spreader 530 , slider switch 515 , and scalpel 520 are substantially the same as those same items shown and explained relative to tool 400 shown in FIGS. 12A-12E .
- the housing 505 of the device of FIGS. 13A-13C is curved shaped to ergonomically fit in the palm of a person's hand.
- the housing 505 includes a flip tab 15 positioned to rotatably open a storage hatch 20 about a rotatable hinge 25 for accessing a storage compartment 30 for retention of tissue preparation components such as prep-wipes 40 , retainer strap 35 for endotracheal tube stabilization, and access to a standard 6 mm endotracheal breathing tube 45 (see also FIGS. 2A-2F ) that is positioned within a tube cavity 50 formed within the housing 10 .
- tissue preparation components such as prep-wipes 40
- retainer strap 35 for endotracheal tube stabilization and access to a standard 6 mm endotracheal breathing tube 45 (see also FIGS. 2A-2F ) that is positioned within a tube cavity 50 formed within the housing 10 .
- cuff retainers 55 ( a ), 55 ( b ) having retainer strap slits 56 ( a ), 56 ( b ) positioned on opposite sides of the endotracheal tube 45 may be made available to assist the user in removing the endotracheal tube 45 from the tube cavity 50 .
- the cuff retainers 55 ( a ), 55 ( b ) extend outside of the housing 10 .
- other features of the device 500 may include a plurality of detents 85 ( a )-( c ) positioned at prescribed intervals, scalpel distance demarcations 90 ( a )-( c ) (indicating distances of 5 mm, 10 mm, and 15 mm), pushbutton 95 , 96 activation and verification of IR and visible light spectrum LEDs 100 , 105 mounted on the front-underside of the housing 505 .
- Recessed areas 535 may be provided on each side of the housing 505 for grip and hook finger tab compression of each of the tissue spreader legs 460 A, 460 B.
- each leg 460 A, 460 B rotates approximately 20+ degrees ( FIG. 14B ).
- an LED lens 540 may be provided having an integrally molded locating support boss 545 for rotating the depth guard/“hook”/tissue spreader 530 and further includes detents 550 for identifying the plurality of angle openings for each leg 460 A and 460 B.
- FIGS. 15A-15F show a compact, hand-held, ergonomically designed, stand-alone device 600 having a combination tracheal “hook” 605 and tissue-spreader/dilator 610 integrally formed therein.
- the combination tool 600 is of a generally durable, sterilizable, single-piece injection molded construction.
- the combination device 600 includes an elongated body 615 having a tracheal “hook” 605 at one end and a curved “trosseau” style dilator 610 with a bifurcated “slide-ratchet” track 620 for opening and closing the dilator or tissue spreader tips or tines 625 A, 625 B positioned at the opposite end of the device 600 .
- the “slide-ratchet” track 620 may further include an actuator handle 630 , a “scissors” shaped gripping means in one embodiment, having an attached post 635 for operable engagement with the track 620 to incrementally open and close the dilator 610 .
- the post 635 provides for ratcheted/notched engagement of the actuator handle 630 with corresponding detents or notches 640 positioned along opposite sides 645 , 646 of the bifurcated track 620 .
- the handle 630 is moved along the track 620 in one direction the dilator 610 is incrementally opened.
- the dilator 610 is incrementally closed.
- the overall length of the device 600 is approximately 5.5 inches ( FIG. 15A ), while the closed or “neutral” static state width of the dilator 610 is approximately 0.130 inches ( FIG. 15B ) and the maximum opened state of the dilator is approximately 0.625 inches ( FIG. 15C ).
- the closed or “neutral” static state width of the dilator 610 is approximately 0.130 inches ( FIG. 15B ) and the maximum opened state of the dilator is approximately 0.625 inches ( FIG. 15C ).
- FIGS. 16-19 show another embodiment of a durable, compact, lightweight, ergonomic hand-held device having universal and common components and methodology of execution for use in, among other things, one-hand operation in providing an opening into the body such as in establishing an airway in medical procedures.
- the device 700 includes a housing 705 having first and second sidewalls 706 a , 706 b connected or joined together along a centerline for housing therebetween various elements of the device 700 .
- the device 700 further includes a first slider unit 710 for extending and retracting a scalpel 711 , and a second slider unit 720 for extending and retracting a bifurcated tissue spreader 721 .
- the scalpel 711 is operably connected to its respective slider unit 710 by well-known means such as those methods use to retain the blade of a box cutter.
- the scalpel may include an orifice or cutout (not shown) for mating with a correspondingly shaped protrusion 719 formed in the first slider unit 710 .
- the bifurcated tissue spreader 721 includes a first elongated arm 722 and a second elongated arm 723 each having a hollow barrel 722 a , 723 a formed at one end of the respective first and second elongated arms 722 , 723 .
- the hollow barrels 722 a , 723 a are position atop each other and between upper and lower portions of a “C” section 724 formed in the second slider unit 720 where a retaining pin 726 positioned through the hollow barrels 72 a , 723 a holds the first and second elongated arms 722 , 723 of the tissue spreader 721 in place in the second slider unit 720 .
- first and second elongated arms 722 , 723 of the tissue spreader 721 may each include a “hooked” distal portion 717 a , 717 b.
- the scalpel 711 and tissue spreader 721 are disposed or stored safely and conveniently within the housing 705 .
- the first slider unit 710 and the second slider unit 720 are positioned within a slider track 730 formed in the first and second sidewalls 706 a , 706 b .
- the slider track 730 permits the scalpel 711 and tissue spreader 721 to be extended away from the housing 705 and retracted toward the housing 705 .
- the device 700 described herein provides for retractable deployment, i.e., extension and retraction of a scalpel 711 and a tissue spreader 721 along a common slider track 730 .
- the first or scalpel slider unit 710 is positioned forward of the second or tissue spreader slider unit 720 within the slider track 730 for retractable deployment from the same side/end (first end 707 a ) of the device 700 .
- a spring or similar tensioning device 725 is operably connected to the first slider unit 710 along a hooked protrusion 727 and to one of the first or second sidewalls 706 a , 706 b to apply tension to the first slider switch 710 while in the extended position.
- the first slider unit 710 is moved along the slider track 730 to extend and lock the scalpel 711 into position from the housing 705 .
- the second slider unit 720 is then moved along the slider track 730 in the same direction and as the first slider switch 710 to auto-retract the scalpel 711 while simultaneously extending and spreading the bifurcated tissue spreader 721 .
- auto-retract is understood to mean that a single action (movement of the second slider unit 720 and its corresponding tissue spreader 721 ) causes a second action (retraction of the first slider unit 710 and its associated scalpel 711 ) to occur.
- movement of the second slider unit 720 further causes a third action, that is, the spreading apart of the arms 722 , 723 of the tissue spreader 721 to occur.
- a third action that is, the spreading apart of the arms 722 , 723 of the tissue spreader 721 to occur.
- the structural configuration and positioning of the first slider unit 710 and the second slider unit 720 on the same slider track 730 results in a “cause and affect” relationship between the two units 710 , 720 without any need for further manipulation, adjustment, movement, etc., from any other structural element.
- movement of the second slider unit 720 causes the first slider unit 710 to retract as a result of the attached spring ( 725 ) returning to its normal “relaxed” state.
- the housing 705 also provides for switch and/or pushbutton 735 , 736 activation and verification of IR (infrared) and visible light spectrum LEDs 740 , 741 mounted on the front-underside of the housing 705 .
- Lithium ion batterie(s) 728 are positioned within the housing 705 to provide power to the LEDs 740 , 741 .
- the pushbuttons 735 , 736 and batteries are electrically connected to the LEDs 740 , 741 via a printed circuit board (PCB) or ribbon 737 , as shown in FIG. 17 .
- PCB printed circuit board
- “Gripper nubs” (raised bumps) 745 may be molded into the housing 705 or formed from rubber and applied to the housing 705 to provide a textured surface to assist the user in holding, gripping, or otherwise maneuvering the device 700 .
- the device 700 may further include an elongated carriage 750 formed from the joined together sidewalls 706 a , 706 b of the device 700 and a protruding clip 755 each extending from a second end 707 b opposite the first end 707 a of the device 700 .
- the protruding clip 755 is positioned in close proximity to the underside of the sidewalls 706 a , 706 b such that prep wipes (not shown) may be retained between the protruding clip 755 and the underside of the sidewalls 706 a , 706 b.
- the elongated carriage 750 having spaced apart sides 751 a , 751 b and the protruding clip 755 form or define an open-well or compartment 765 for retaining an airway tube 770 ( FIG. 16 ) and sterile gaze (not shown).
- the carriage 750 further includes a curved distal portion 752 formed by the spaced apart sides 751 a , 751 b .
- the distal portion 752 of the carriage 750 is shaped to correspond to the shape of the airway tube 770 retained therebetween and may further be configured to allow the distal portion 752 , i.e., spaced apart sides 751 a , 751 b to flex apart and return to their original position due to material memory to assist in holding one end of airway tube 770 in place.
- a retaining or mounting stem 775 having an O-ring 780 positioned around the mounting stem 775 may further be including and positioned along an upper area 776 of the device 700 to assist in holding the opposite end of the airway tube 700 in place.
- the device 700 includes a first slider unit 710 for extending and retracting a scalpel 711 , and a second slider unit 720 for extending and retracting a bifurcated tissue spreader 721 along a common slider track 730 formed between first and second sidewalls 706 a , 706 b of the housing 705 to permit for retractable deployment and retraction of a scalpel 711 and a tissue spreader 721 from the same side of the device 700 .
- the first slider unit 710 having the scalpel 711 attached thereto is moved in a forward direction along the slider track 730 to extend the scalpel 711 from the housing 705 .
- the first slider unit 710 is movably retained within an elongated top rail 786 a and a corresponding elongated bottom rail 786 b of the slider track 730 formed in each of the first and second sidewalls 706 a , 706 b to permit movement of the first slider switch 710 along the slider track 730 until the first slider unit 710 is position between an upper forward portion 785 a of the top rail 786 a and a bottom forward portion 785 b of the bottom rail 786 b of each side the slider track 730 , and a retaining nub 787 ( FIG.
- the first slider unit 710 is retained in the forward position, despite tension from the spring 725 having been extended due to the forward movement of the first slider unit 710 along the slider track 730 , by an “L” shaped retaining lip 788 located at one end of the first slider unit 710 being positioned against the retaining nubs 787 .
- the curved surface of the retaining nubs 787 permits the retaining lip 788 to be easily pushed passed the retaining nubs 787 when moved in a forward direction, but held relatively securely when attempting to move in the backward or rearward direction by a relatively flat surface back surface of the retaining lip 788 .
- the first slider unit 710 is retained in the forward position along the slider track 730 with the scalpel 711 extended.
- the second slider unit 720 is moved in the forward direction to extend and expand the first elongated arm 722 and the second elongated arm 723 of the bifurcated tissue spreader 721 , and to facilitate auto-retraction/release of the first slider unit 710 .
- the second slider switch 720 is movably retained within the elongated top rail 786 a of the slider track 730 formed in each of the first and second sidewalls 706 a , 706 b to permit movement of the second slider unit 720 along the slider track 730 .
- the first elongated arm 722 and the second elongated arm 723 of the bifurcated tissue spreader 721 are retained within the “C” section 724 formed in the second slider unit 720 .
- the first elongated arm 722 and the second elongated arm 723 of the bifurcated tissue spreader 721 are further positioned such that one of the elongated arms 722 , 723 extends from inside the housing 705 through a first window 790 a formed in one of the sidewalls 706 a , 706 b , and the other elongated arm 722 , 723 extends from inside the housing 705 through a second window 790 b opposite the first window 790 a to position each of the elongated arms 722 , 723 on opposite sides of the device 700 .
- a second lateral sidewall portion 795 b formed between the top rail 786 a and the bottom rail 786 b of the slider track 730 of the second sidewall 706 b force the first elongated arm 722 and the second elongated arm 723 apart ( FIG.
- first and second lateral sidewall portions 795 a , 795 b approach the “C” section 724 formed in the second slider unit 720 (connection point of the first elongated arm 722 and the second elongated arm 723 of the bifurcated tissue spreader 721 ).
- the first and second elongated arm 722 , 723 are displaced or spread apart approximately 13 mm.
- first and second elongated arms 722 , 723 are moved along and therefore spread apart by the respective first and second lateral sidewall portions 795 a , 795 b a first indented portion 796 a of the first elongated arm 722 contacts a first protrusion 797 a formed on the first lateral sidewall portion 795 a .
- a second indented portion 796 b of the second elongated arm 723 contacts a second protrusion (not shown) formed on the second lateral sidewall portion.
- the bifurcated tissue spreader 721 is retained in this forward position by a first elongated tension strip 798 a formed in the first sidewall 706 a and biased against the first elongated arm 722 , and a second elongated tension strip 798 b formed in the second sidewall 706 b and biased against the second elongated arm 723 .
- Movement of the second slider unit 720 in the backward or rearward direction is accomplished by manually applying sufficient force to the second slider unit 720 in the backward direction to overcome the bias force applied by the first and second elongated tension strips 798 a , 798 b.
- forward movement of the second slider unit 720 facilitates auto-retraction of the first slider unit 710 .
- a curved shaped lower segment 799 of the “C” section 724 of the second slider unit 720 contacts and forces the retaining lip 788 of the first slider unit 710 to disengage from the retaining nubs 787 as the second slider unit 720 moves past the retaining lip 788 forcing the retaining lip 788 downward to permit the spring 725 to move the first slider unit 710 back to its original position within the housing 705 with the scalpel 711 safely retracted ( FIG. 20D ).
- Forward and backward directional movement of the second slider unit 720 may be accomplished independent of the first slider unit 710 and may be accomplished regardless of the position of the first slider unit 710 along the slider track 730 .
Abstract
Description
- This application claims priority under 35 U.S.C. §120 to provisional application No. 60/923,856 filed on Apr. 17, 2007, the contents of which are incorporated by reference in their entirety.
- The disclosure relates generally to a surgical instrument such as an apparatus and method for providing a passage into the body, and more particularly, the disclosure relates to a percutaneous or a non-dissection apparatus and method for use in, among other things, establishing an airway in medical procedures including tracheostomies and cricothyroidectomies.
- In certain patient care situations, a first responder must immediately establish and maintain a patient's airway. Once an airway is established, the first responder must determine whether the patient is breathing. If breathing is adequate, maintenance of the airway should be continued. If breathing is inadequate, or absent, artificial respiration should be initiated.
- Depending on among other things, the type and extent of an injury, various procedures and devices are available to assist in establishing an airway. Relatively less intrusive techniques for establishing an airway typically used in the absence of trauma include the head-tilt/chin-lift maneuver. With suspected trauma and/or an unconscious patient, a modified jaw thrust technique may be more appropriate to open the airway. Other methods for establishing an airway include the insertion of a nasopharayngeal airway, or in the case of a potentially life-threatening situation such as a complete upper airway obstruction the patient may require a tracheotomy or cricothyrotomy.
- In this regard, a tracheotomy is generally defined as a temporary or permanent treatment for a variety of causes of breathing difficulties in which the creation of a new breathing pathway is required to by-pass the nose, mouth, and upper throat. A tracheotomy is usually considered when an endotracheal (ET) tube (a tube that goes in the throat through the mouth) will not be effective (in some emergency situations for example), or would be required for a long time. Sometimes, a tracheotomy is performed when an ET tube cannot be placed due to narrowing of the windpipe, blockage of the voice box (larynx) or facial trauma prevents intubation via the ET tube.
- When an airway must be created immediately, a slightly different procedure called a cricothyroidotomy may be done. A cricothyrotomy (also called thyrocricotomy, cricothyroidotomy, inferior laryngotomy, intercricothyrotomy, coniotomy or emergency airway puncture) is an emergency incision through the skin and cricothyroid membrane to secure a patient's airway for emergency relief of upper airway obstruction. A cricothyrotomy is usually performed by paramedics and emergency physicians as a last resort in cases of severe choking due to upper airway obstruction when attempts at orotracheal and nasotracheal intubation have failed.
- Preferably, when establishing an airway by a cricothyroidotomy (sometimes called a tracheotomy), percutaneous or non-dissection devices and techniques are normally preferably to dissection procedures, which require considerable more surgical skills in that many blood vessels are involved which tend to bleed profusely during a dissection procedure.
- In this regard, combat casualty care, (that is, providing cricothyroidectomies in a field environment) continues to be a major challenge. Performing successful cricothyroidectomies has been identified as one of the three most important procedures for saving soldier's lives. Field cricothyroidectomies are critical to maintain life and provide severely injured far-forward battlefield participants an opportunity to survive until treated in a battlefield treatment facility. The current overall complication rate of a combat cricothyrotomy is 32% or 5 times higher than the complication rate when the procedure is conducted under controlled circumstances. Duress, adverse conditions, and non-standardization of airway kits all contribute to a high complication rate, including errors in incision location and incision depth in “combat care situations”.
- In this regard, fast, efficient, reliable, and effective emergency tracheotomies in support of combat casualty care in various field environments are currently not available due to, among other things, (1) lack of adequate and safe lighting, (2) too-deep tissue incisions that open both the trachea and esophageal tissue, (3) lack of device or means to directly and immediately displace incised tissue (4) non-standardization of airway medical kits, i.e., a wide variety of products and components are randomly and individually collected and loosely assembled among a variety of tracheosotomy medical kits (each kit being unique to the individual who assembled the kit), and (5) lack of easy access to necessary kit components.
- The diversity and disparity in medical equipment, lack commonality of procedure/techniques resulting from the use of that equipment, and diminution of needed rapid component access, all contribute to confusion and loss of critical, life-saving time in the execution of emergency cricothyroidectomies in the field.
- A currently available airway device includes the Rusch QuickTrach sold by a number of on-line distributors. Other airway devices include those described in U.S. Pat. No. 4,520,810 issued Jun. 4, 1985 to Weiss; U.S. Pat. No. 4,677,978 issued Jul. 7, 1987 to Melker; U.S. Pat. No. 4,978,334 issued Dec. 18, 1990 to Toye et al.; and U.S. Pat. No. 5,217,005 issued Jun. 8, 1993 to Weinstein, and the common #11 surgical scalpel and well-known endotracheal breathing tube.
- Although each of the aforementioned devices provide for an airway into the body, none of the devices provide the combination of features of the subject matter described herein. Accordingly, it is desirable to provide a method and apparatus having universal and common components and safer and more expedient methodology of execution in providing an airway in medical procedures including tracheostomies and cricothyroidectomies under all emergency medical circumstances and environments.
- The subject matter described herein relates generally to a surgical instrument such as an apparatus and method for providing a passage into the body and displacement (spreading) of incised tissue, and more particularly, to a percutaneous or a non-dissection apparatus and method having universal and common components and methodology of execution for use in, among other things, establishing an airway in medical procedures including tracheostomies and cricothyroidectomies.
- In one embodiment, the device described herein for providing a passage into the body includes, a housing, and a scalpel and a tissue spreader disposed within the housing along a common slider track for extension and retraction (deployment) of the scalpel and the tissue spreader from the same side of the housing. The tissue spreader includes a bifurcated leading edge formed by a first arm and a second arm, and configured to move from a closed position to an open position upon retractable deployment of the tissue spreader to open a site of incision for acceptance of a breathing tube.
- In another embodiment, an apparatus for providing a passage into the body, comprises a housing; a slider track formed within the housing; and a first slider unit configured to retain a scalpel and a second slider unit configured to retain a tissue spreader each operably connected to the slider track for movement along the slider track.
- In still another embodiment, an apparatus for providing a passage into the body includes a first slider unit and a second slider unit operably connected to a slider track for retractable deployment of a scalpel and a tissue spreader attached respectively thereto, and for the auto-retraction of the scalpel due to movement of the second slider unit.
- Furthermore, the device described herein for establishing an airway, provides, among other things, (1) visible and infra-red light sources, (2) a combination of a clean retractable scalpel and a tissue spreader device, (3) incision depth gauging and regulation, (4) tissue preparation and administration components, (5) an endotracheal tube, and (6) a tube stabilization device all integrated into a durable, compact, lightweight, ergonomic hand-held device for one-hand operation (7) integrated tissue “hook” (commonly known and referred to as a “trach hook” for additional means of displacing incised tissue.
- These and other embodiments will become readily apparent to those skilled in the art from the following detailed description of the various embodiments having reference to the attached figures, the subject matter described herein not being limited to any particular preferred embodiment(s) disclosed.
-
FIG. 1A shows one embodiment of a durable, compact, lightweight, ergonomic hand-held device having universal and common components and methodology of execution for use in, among other things, one-hand operation in providing an opening into the body such as in establishing an airway in medical procedures including tracheostomies and cricothyroidectomies. -
FIGS. 1B-1C show cutaway views of the apparatus shown inFIG. 1A . -
FIGS. 2A-2F illustrate one method of performing or executing an emergency tracheotomy (cricothyroidectomy) utilizing the device described herein. -
FIG. 3 shows tracheal and associated tissue depths for selected persons, and proposed scalpel depth information for retractable deployment of the scalpel. -
FIGS. 4A-4E show various views of the device shown inFIG. 1A , and more particularly, show the same-side retractable deployment relationship of a scalpel and a tissue spreader along a common slider track in accordance with one embodiment (FIG. 4E ), and an opposite side retractable deployment relationship of a scalpel and a tissue spreader along a common slider track in accordance with another embodiment (FIG. 4D ). -
FIGS. 5A-5B show movement of the slider switch and corresponding tissue spreader switch along the slider track to an extension depth of 10 mm. -
FIGS. 6A-6B are similar toFIGS. 5A-5B and show movement of the slider switch and corresponding tissue spreader switch along the slider track to an extension depth of 15 mm. -
FIGS. 7A-7B show movement of the slider switch and corresponding tissue spreader switch along the slider track to an extension depth of 20 mm. -
FIGS. 8A-8E show top, side, side with “Quick Trach” cartridge inserted and withdrawn from a housing, back, and front views, respectively of an alternative embodiment of a device in accordance with an embodiment. -
FIGS. 9A-9L show various views of one embodiment having a removably attached combination tracheal “hook” and tissue-spreader tool. -
FIGS. 10A and 10B shows a general-purpose tool for providing a passage into the body in accordance with one embodiment. -
FIG. 11A is top view of the tool of the tool shown inFIGS. 10A and 10B showing a scalpel extended between an elongated slit formed in the “hooked” protrusion. -
FIG. 11B andFIG. 11C respectively show side views of the tool with the scalpel in an extended and retracted position. -
FIG. 11D shows a front view of the tool including a first extension and a second extension of a bifurcated end, the “hooked” protrusion with its elongated slit, and the scalpel. -
FIG. 11E shows a side view of the tool with the sides of the tool body removed to show the connection between the slider switch and the scalpel. -
FIG. 11F shows the bifurcated end of the tool and illustrates a general range of motion of the tissue spreader. -
FIGS. 12A-12E show an apparatus for providing a passage into the body in accordance with another embodiment. -
FIGS. 13A-13C andFIGS. 14A-14D show an apparatus for providing a passage into the body in accordance with still another embodiment. -
FIGS. 15A-15E show an apparatus for providing a passage into the body in accordance with still another embodiment. -
FIGS. 16-19 and 20A-20D show an apparatus for providing a passage into the body in accordance with still another embodiment. - Embodiments of the will now be described with references to the accompanying Figures, wherein like reference numerals refer to like elements throughout. The terminology used in the description presented herein is not intended to be interpreted in any limited or restrictive manner, simply because it is being utilized in conjunction with a detailed description of certain embodiments. Furthermore, various embodiments (whether or not specifically described herein) may include novel features, no single one of which is solely responsible for its desirable attributes or which is essential to practicing the subject matter herein described.
- As used herein the terms tracheotomy and cricothyroidotomy, and any form of each word, are considered to be interchangeable for purposes of explaining the subject matter provided herein.
- Generally, in one embodiment, the device described herein provides for a compact universal cricothyrotomy (CRIC) kit that is relatively safer, more efficient, consistent, and easier to use when executing or providing an opening into the body, such as when performing an emergency tracheotomy, in all environments, including dark and “hot” combat theater situations, when compared to known emergency tracheotomy devices.
- The device provides, among other things, (1) visible and infra-red light sources, (2) a combination of a clean retractable scalpel and a tissue spreader device, (3) incision depth gauging and regulation, (4) tissue preparation and administration components, (5) a standard (6 mm) endotracheal tube, and (6) tube stabilization device all integrated into a durable, compact, lightweight, ergonomic hand-held device for one-hand operation in establishing an airway.
-
FIG. 1A shows a side view of one embodiment of the device orCRIC kit 5. As shown in the figure, this embodiment of thedevice 5 includes a curved ergonomicallyshaped housing 10 designed to fit in the palm of a person's hand. In one embodiment, thehousing 10 is constructed from molded plastic such as a polycarbonate, polypropylene, etc. The further use of other plastics, as well as other materials such as metals, composites, glass, rubber, and the like, in the construction of the device will depend on a number of factors including, for example, material cost, durability, and the intended use of a part. - Among other things, the
housing 10 includes aflip tab 15 positioned to rotatably open astorage hatch 20 about arotatable hinge 25 for accessing astorage compartment 30 for retention of tissue preparation components such as prep-wipes 40,retainer strap 35 for endotracheal tube stabilization, and access to a standard 6 mm endotracheal breathing tube 45 (see alsoFIGS. 2A-2F ) that are positioned within atube cavity 50 formed within thehousing 10. When thestorage hatch 20 is in the open position (FIG. 2A ) cuff retainers 55(a), 55(b) having retainer strap slits 56(a), 56(b) positioned on opposite sides of theenodtracheal tube 45 are available to assist the user in removing theendotracheal tube 45 from thetube cavity 50. When thestorage hatch 20 is in the closed position (FIG. 2B ) the cuff retainers 55(a), 55(b) extend outside of thehousing 10. - As shown in
FIG. 1B andFIG. 1C , thehousing 20 further includes afirst slider switch 60 for extending and retracting a scalpel 65 (FIG. 2C ), and asecond slider switch 70 for extending and retracting atissue spreader 75. In this regard, thescalpel 65 andtissue spreader 75 are operably connected to respective slider switches 60, 70 by well-known means such as those methods used to extend and retract the blade of a box cutter. - In a retracted position the
scalpel 65 andtissue spreader 75 are disposed or stored safely and conveniently withinhousing 10. Thefirst slider switch 60 andsecond slider switch 70 are positioned within aslider track 80 for extending and retracting thescalpel 65 andtissue spreader 75 away from thehousing 10 and toward thehousing 10. In other words, in one embodiment, the device described herein provides for retractable deployment of ascalpel 65 and atissue spreader 75 along acommon slider track 80. - In the embodiment shown in
FIGS. 1A-1C , the first orscalpel slider switch 60 is positioned forward of the second or tissuespreader slider switch 70 within theslider track 80 for retractable deployment from the same side of thedevice 5. - In an alternative embodiment shown in
FIG. 4D , the first orscalpel slider switch 60 is positioned to retractably deploy from one end of thedevice 5 while the second or tissuespreader slider switch 70 is positioned to retractably deploy from the opposite end of thedevice 5. Likewise, in this embodiment asingle slider track 80 or dual slider tracks (not shown) may be utilized for retractable deployment of thefirst switch 60 andsecond switch 70. - The
slider track 80 may include a plurality of detents 85(a)-(c) positioned at prescribed intervals to provide incision-deep regulation, gauging, and feedback to the user as to the extended or retracted distance of the scalpel 65 (seeFIG. 5A ). Scalpel distance demarcations 90(a)-(c) may also be provided for incision-depth regulation and gauging by visual verification and confirmation of thescalpel 65 extension or retraction distance. In one example, verification of scalpel distance positioning is provided by markings such as 10, 15, and 20 millimeters molded directly into thehousing 10. These markings 90(a)-(c) confirm the scalpel positioning as provided by the detents 85(a)-(c) on the associatedslider track 80. - Accordingly, as shown in
FIGS. 5A , 6A, and 7A, as thescalpel switch 60 is moved from left to right in each of the figures from a first detent position 85(a) to a second and a third detent position 85(b), 85(c), thescalpel 65 is moved outward from thehousing 10 approximately 10 mm, 15 mm, and 20 mm. - As further shown in
FIG. 1C , thehousing 10 also provides for switch and/orpushbutton housing 10.Lithium ion batteries 110 are housed within thehousing 10 to provide power to the LEDs 100, 105. “Gripper nubs” (raised bumps) 115 may be molded into thehousing 10 or formed from rubber and applied to thehousing 10 to provide a textured surface to assist the user in holding, gripping, or otherwise maneuvering thedevice 5. - As shown in
FIGS. 2A-2F , thedevice 5 is a relatively simple, safe, and easy to use device. In one method, use of thedevice 5 to establish an airway in medical procedures, including tracheostomies and cricothyrotomies, begins by opening thestorage hatch 20, removing one or more prep-wipes/pads 40, and wiping the intended site or area ofincision 120 for establishment of an airway. As shown inFIG. 2B , thestorage hatch 20 is closed and depending on the lighting conditions either the IR LED light 100 or visible-spectrum LED light 105 may be activated by the associated single pushbutton membrane or switch 95, 96 to illuminate the site ofincision 120. As shown inFIG. 2C , establishing an airway then proceeds by deploying or extending the scalpel 65 a predetermined distance (10 mm, 15 mm, or 20 mm) as indicated by the scalpel demarcations 90(a)-(c) and/or the detents 85(a)-(c). - In this regard, in the embodiment shown in
FIGS. 4A-4C , and 4E, thedevice 5 provides for safe extension and retraction (deployment) of thescalpel 65 by a half-circle slider switch 60 moved along aslider track 80 having detents 85(a)-(c) position to indicate thescalpel 65 extension and retraction distances of 10 mm, 15 mm, and 20 mm from thehousing 10, as well as the extension and retraction of an associatedtissue spreader 70 by a corresponding half-circle slider switch 70. - As shown in
FIG. 3 , the 10, 15, and 20 millimeter depth of thescalpel 65 is generally shown as approximating the centerline depth of the trachea for 50% of certain individuals. For example, persons 6-8 years old generally require an incision depth of 10 mm, soldiers a depth of 15 mm, and overweight adults a depth of 20 mm. Accordingly, once the patient has been assessed for size and categorized as to trachea centerline depth, extension of thescalpel 65 to the appropriate depth ensures adequate penetration through the outer skin (epidermis), cricocartilage, and anterior wall of the trachea, while preventing too-deep penetration of thescalpel 65 that could potentially cause damage to the posterior tracheal inner surface. In regard toscalpel 65 extension, the front of the housing 125 (i.e., the part of the housing directed toward the site of incision) acts as a buffer or barrier to prevent further movement of thescalpel 65 into the trachea cavity that may result in excessive penetration of thescalpel 65 beyond the selected penetration/extension depth 85(a)-(c), which results in damage to the trachea wall and/or other vital areas such as the esophagus. Persons of ordinary skill in the art will understand that other scalpel depths may replace and/or supplement those indicated above. - As shown in
FIG. 2D , and more specifically in the sequence of illustration shown inFIG. 4E , after an incision is made with thescalpel 65, thetissue spreader 75 is extended forward along theslider track 80 using a half-circle slider switch 70 similar to the half-circle slider switch 60 used to extend thescalpel 65 forward. In this regard, the half-circle tissuespreader slider switch 70 is brought forward to mate with the half-circlescalpel slider switch 60. Mating of thetissue spreader switch 75 with thescalpel switch 60, is further shown inFIGS. 5B , 6B, and 7B at 10 mm, 15 mm, and 20 mm, respectively along theslider track 80. - Movement of the tissue
spreader slider switch 70 along theslider track 80 until it mates with thescalpel slider switch 60 permits a bifurcated taperedleading end 130 of thetissue spreader 75 to: (1) slide forward in a “closed” position “hugging” thescalpel 65, (2) to eventually penetrate into the tracheal cavity through the incision created by thescalpel 65, and (3) to move from the “closed” position to an “open” position to spread the incision to an approximate distance of 1.27 centimeter (0.5″) to allow room for insertion of thebreathing tube 45. Persons of ordinary skill in the art will understand that thedevice 5 may be designed so that the tissue spreading distance may vary from the distance stated above to accommodate other size tubes or similar articles for maintaining an airway. - As further shown in
FIG. 4E , opening or spreading of the scalpel's bifurcatedleading edge 130 is facilitated by the enlarged distal end 135 (i.e., that end of scalpel opposite the cutting end 140) of thescalpel 65 positioned between afirst arm 140 and asecond arm 141 of thetissue spreader 75. In this regard, as thetissue spreader 75 is moved forward along theslider track 80 the enlargeddistal end 135 ofscalpel 75 forces the tapered trailingend 145 of thetissue spreader 75 apart, resulting in a similar spreading apart of theleading end 130 of thetissue spreader 75. Mating of thetissue spreader switch 70 with thescalpel switch 60 acts to regulate and correspond the depth oftissue spreader 75 penetration into the incision opening with the depth ofscalpel 65 penetration into the incision opening. As shown inFIG. 4E , retractable deployment distance of the tissue spreader is such that thetissue spreader 75 extends beyond the retractable deployment distance ofscalpel 65 to permit insertion of theendotracheal breathing tube 45 into the incision site without removal of thetissue spreader 75 from the incision. - As shown in
FIG. 2E andFIG. 2F , once the incision is spread open to a diameter of approximately 1.27 cm by thetissue spreader 75, theendotracheal tube 45 and endotracheal tube retainer or tie-downstrap 35 are removed from thestorage compartment 30. Theendotracheal tube 45 is then inserted between the bifurcated leadingend 130 of thetissue spreader 75 and into the incision opening. The device 5 (including the tissue spreader 75) is retracted or removed from the incision, and the endotrachealtube retainer strap 35 is attached toendotracheal tube 45 along the cuff retainer slits 56(a)-(b) and tied around the patient's neck to secure theendotracheal tube 45 in place. - An alternative embodiment of the
device 5 is shown inFIGS. 8A-8E . In this embodiment, thedevice 145 includes areusable housing 150 with a butterfly-opening latch 147, and a slidable cartridge housing 146 that moves and deploys the inserted disposable/replaceablepro-trach cartridge 155 temporarily retained therein for storage and deployment in establishing an airway. Thecartridge 155 includes acombination piercing tube 156 surrounding by asleeve 157. Astorage compartment 160 is provided to retain an industry standard 12 mmbreathing tube adaptor 170. Thebreathing tube adapter 170 is attached to thesleeve 157 to maintain establishment of the airway. Accordingly, one method of establishing an airway using the device shown inFIGS. 8A-8E includes, bringing the piercingtube 156 and associatedsleeve 157 forward byslide switch tube 156, and inserting thesleeve 157 into the site of incision by the continued forward movement of thecombination piercing tube 156 andsleeve 157. - After insertion of the
sleeve 157 into the incision site, thesleeve 157 and piercingtube 156 are released from thehousing 150 by thebutterfly latch 147 to remain disposed within the incision site. In this regard, thehousing 150 is made available for accepting another similarly constructedpro-trach cartridge 155 therein for use in establishing an airway. The 12 mmbreathing tube adaptor 170 is then removed from thestorage compartment 160, attached to thesleeve 157 by threading, friction fit, or a similar attachment means, and retained in place to maintain establishment of the airway. - As shown in
FIGS. 9A-9L , thedevice 5 may further include a removably attached combination tracheal “hook” and tissue-spreader tool 200. Thecombination tool 200 is of a general durable, sterilizable, single-piece injection molded, translucent polycarbonate material construction. Although the length of thecombination tool 200 may vary, acombination tool 200 length of approximately 4.5 inches is typically adequate for most applications. The shape ofcombination tool 200 corresponds to the shape of thehousing 10 so that when placed in a closed or retracted position (explained below) thetool 200 stores directly onto theCRIC housing 10. - As shown in at least
FIGS. 9C-9F , thecombination tool 200 includes afirst end 201 having a “hook” shapedtip 202, and a bifurcated second end 203 (opposite the first end 201) having afirst leg 204A and asecond leg 204B biased in a normally open position. Thecombination tool 200 further includes afirst extension 205A positioned on oneleg 204A of thebifurcated end 203, and asecond extension 205B positioned on theother leg 204B of thebifurcated end 203. As shown in comparingFIG. 9C toFIG. 9F , the shape of thefirst extension 205A andsecond extension 205B may vary to facilitate compression or closing of the bifurcatedsecond end 203. - Furthermore, a dual-purpose a
first stem 206A is positioned at the tip of oneleg 204A and a dual-purposesecond stem 206B is positioned at the tip of theother leg 204B. Eachextension combination tool 200. As further shown in comparingFIG. 9C toFIG. 9F , the shape of thefirst stem 206A andsecond stem 206B may likewise vary to facilitate the necessary spreading of tissue as intended by the bifurcatedsecond end 203. In this regard, in one embodiment, the opening between thelegs bifurcated end 203 of thecombination tool 200 in a relaxed state (shown inFIG. 9F ) has an inside diameter of approximately 0.625 inches and an outside diameter of approximately 0.75 inches. Further in this regard, in one embodiment, the opening between thelegs 204, 204B of thebifurcated end 203 of thecombination tool 200 in a compressed state (shown in Figure H) is approximately 0.13 inches. - In one embodiment,
protrusions housing 10 of thedevice 5 for removably receiving an associatedstem combination tool 200 onto thehousing 10. In this regard, force applied in the direction of arrows “A” (FIG. 9C ) to the first andsecond extensions protrusions holes second extensions second end 203 to move in the direction of arrow “B” (FIG. 9C ), biasing thesecond end 203 to the open position, and permitting the stems 206A, 206B to be removably received into the locatingholes - Once the first and second lateral stems 206A, 206B are positioned inside the locating
holes combination tool 200 is capable of being rotated approximately 180 degrees from a closed or retracted position (FIG. 9A ) to an open or extended position (FIG. 9B ). Preferably, a retainingclip 215 having detents (not shown) formed therein is molded into thehousing 10 to further assist in retaining thecombination tool 200 by holding, gripping, or otherwise securing thefirst end 201 ofcombination tool 200 while in the closed position. In one embodiment, thehousing 10 is molded to include a “sheath” likestorage extension 220 for protecting the “hook” shapedtool 202 during storage of thecombination tool 200. In this regard, the “sheath” likeextension 220 may be constructed to include the retainingclip 215 mention above, or a trough of reduced width may be included to frictionally secure thefirst end 201 of thecombination tool 200. - In practice, the
combination device 200 may remain attached to thehousing 10 and rotated into the extended position so that the “hook” shapedtip 202 of thefirst end 201 may be inserted into a previously made incision in the tissue. The tissue may then be distended by moving thedevice 5 with attached “hook” in direction “C” (FIG. 9C ) so the incision and/or tissue may be irrigated, for example. - Alternatively, as detailed above, the
combination device 200 may be removed from thehousing 10 and used independently as a stand alone tool or in conjunction with the various design features of thedevice 5 explained above. In this regard, the lateral stems 206A, 206B of the bifurcatedsecond end 203, previously used to rotatably retain thecombination device 200 to thehousing 10, are made available for insertion into an incision. Preferably, when biased to the open position, the bifurcatedsecond end 203 spreads the tissue apart a minimum of 6 mm to accommodate a standard sizeendotracheal tube 45 or similar device. - Variations of the combination tool shown in at least
FIGS. 9C and 9F include modifications to the length and shape of the space oropening 230 extending between theopposite legs bifurcated end 203 to facilitate spreading of the legs ortines combination tool 200. - In still another embodiment, as shown in
FIGS. 10A and 10B , the device may be embodied in the form of a general-purpose tool 300 for providing a passage into the body. In this regard, thetool 300 includes atool body 305, preferably of a one-piece molded construction, having anelongated slider track 310 formed therein. - The
tool 300 preferably further includes aslider switch 315 movably disposed within theslider track 310 for extending and retracting ascalpel 320 from afirst side 325 of thetool body 305. In the retracted position thescalpel 320 is housed betweenopposite sides tool body 305. In this regard, with thescalpel 320 in the retracted position thetool body 305 may be “safely” handled, carried, or otherwise manipulated as thescalpel 320 is stored within thetool body 305. In this embodiment, thetool body 305 may be constructed of a semi-translucent material, such as plastic, to provide visual assessment of thescalpel 320 position as well as the tissue area of the patient. - As shown in
FIG. 10A , thetool body 305 further includes a “hook” shapedprotrusion 321 extending from thesame side 325 of thetool body 305 as thescalpel 320 when thescalpel 320 is in an extended position. Theextension 321 includes an elongated slit 322 (FIG. 10B ) generally located in the center of the “hooked”protrusion 321 for receiving thescalpel 320 therethrough when thescalpel 320 is extended from thetool body 305. Theprotrusion 321 functions as a depth guard for thescalpel 320 when making a tissue incision, and as a “hook” 321 for tissue displacement when thescalpel 320 is retracted. In this regard,typical scalpel 320 extension from theprotrusion 321 is generally limited to less than 16 mm. - A
tissue spreader 330 having abifurcated end 335 may be included and located on a second oropposite side 340 of thetool body 305. Thebifurcated end 335 includes afirst leg 360A and asecond leg 360B biased in an open position. Thetool 300 further includes afirst extension 365A positioned on oneleg 360A of thebifurcated end 335, and asecond extension 365B positioned on theother leg 360B of thebifurcated end 335. - Accordingly, in practice, use of the
tool 300 shown inFIG. 10A andFIG. 10B , at least with respect to the “hook” shapedprotrusion 321 and thebifurcated tissue spreader 330 is substantially similar to use of thecombination tool 200 shown inFIGS. 9A-9D above. However, as thetool 300 shown in at leastFIGS. 10A and 10B further includes aretractable scalpel 320, thetool 300 may generally be considered an all or multi-purpose tool for providing a passage into the body. - Other figures, including
FIGS. 11A-11G , show various views of themulti-purpose tool 300 described above. Specifically,FIG. 11A is top view of thetool 300 showing thescalpel 320 extended between theelongated slit 322 formed in the “hooked”protrusion 321. Side views of thetool 300 with thescalpel 320 in an extended and a retracted position are shown inFIG. 11B andFIG. 11C , respectively.FIG. 11D , shows a front view of thetool 300 including thefirst extension 365A and asecond extension 365B of thebifurcated end 335, the “hooked”protrusion 321 with itselongated slit 322, and thescalpel 320.FIG. 11E , is a side view of thetool 300 with thesides tool body 305 removed to show the connection between theslider switch 315 and thescalpel 320.FIG. 11F shows thebifurcated end 335 of thetool 300 and illustrates a general range of motion of thetissue spreader 330. - A further embodiment of a general-
purpose tool 400 for providing a passage into the body is shown inFIGS. 12A-12E . In this regard, many of the design features found in themulti-purpose tool 300 shown in at leastFIG. 10A andFIG. 10B , including atool body 405, aslider track 410 formed therein, and aslider switch 415 disposed within theslider track 410 for extending and retracting ascalpel 420 from afirst side 425 of thetool body 405. However, in contrast to the previously mentioned all-purpose tool 300, this embodiment of thetool 400 includes a depth guard/“hook”/tissue spreader combination 430 integrated into a single device on thesame side 425 of thetool body 405 as thescalpel 420 when extended from thetool body 405. - Accordingly, the
integrated device 430 combines a tissue “hook” 435, incision depth guard 440 (provided by the front face of thetissue hook 435, tissue hook 440), andtissue spreader 445 having abifurcated end 450. Preferably, thebifurcated end 450 includes afirst leg 460A and asecond leg 460B generally biased in a closed position (FIG. 12A ), and a firstrotatable arm 465A connected to thefirst leg 460A and secondrotatable arm 465B connected to thesecond leg 460B for rotatably positioning the first andsecond legs tissue spreader 445 in an open position. In contrast to activation of atissue spreader 75 by a slider switch 70 (see thetool 5 shown at least inFIG. 4A ), activation of the tissue spreader device ofFIG. 12B is provided by therotatable arms tissue spreader leg FIG. 12B . In this regard, rotation of eachrotatable arm tool body 405 opens or spreads thefirst leg 460A andsecond leg 460B of thebifurcated end 450 while rotation of eachrotatable arm tool body 405 closes or brings together thefirst leg 460A and thesecond leg 460B of thebifurcated end 450. - Accordingly, the
combination device 430 allows thescalpel 420 to pass between thelegs tissue spreader 445 to permit an incision to be made in a patient (FIG. 12D andFIG. 12E ). Theincision depth guard 440 maintains ascalpel 420 incision depth of less than 16 mm. Once an incision is made, sequential use of thetissue hook 435 for displacement or distention of the tissue, and tissue spreading utilizing thetissue spreader 445 can take place immediately. Dents 85(a)-(c) such as those explained in conjunction with thetool 5 of at leastFIGS. 5A-7B may be provided on thetool body 405 thereby providing for variable extension depths of thescalpel 420 and/or opening distances of thetissue spreader 445. In one embodiment, the maximum distance between theopen legs - Persons of ordinary skill in the art will understand that any distance/measurement discussed within the detailed description, regardless of whether the distance/measurement refers to some aspect of the scalpel, tissue spreader, or hook, is not meant to be an absolute distance/measurement in that the distance/measurement may vary depending on any number of factors, including the device's intended use.
- Many of the characteristics relating to the various tools for creating a passage into the body, as described herein, may be adapted in another embodiment of the device such as the
device 500 shown inFIGS. 13A-13C and 14A-14D. For example, thedevice 500 includes including ahousing 505, aslider track 510 formed therein, and aslider switch 515 disposed within theslider track 510 for extending and retracting ascalpel 520 from afirst side 525 of thehousing 505. - Likewise, the
housing 500 shown inFIGS. 13A-13C further includes a bifurcated depth guard/“hook”/tissue spreader combination 530 integrated into a single device on thesame side 525 of thehousing 505 as thescalpel 520 when extended from thetool body 505. Persons of ordinary skill in the art will understand that structure, mechanics, functionality, and use of the tissue depth guard/“hook”/tissue spreader 530,slider switch 515, andscalpel 520 are substantially the same as those same items shown and explained relative totool 400 shown inFIGS. 12A-12E . Similar todevice 5 shown at least inFIGS. 1A-1C , thehousing 505 of the device ofFIGS. 13A-13C is curved shaped to ergonomically fit in the palm of a person's hand. - The
housing 505 includes aflip tab 15 positioned to rotatably open astorage hatch 20 about arotatable hinge 25 for accessing astorage compartment 30 for retention of tissue preparation components such as prep-wipes 40,retainer strap 35 for endotracheal tube stabilization, and access to a standard 6 mm endotracheal breathing tube 45 (see alsoFIGS. 2A-2F ) that is positioned within atube cavity 50 formed within thehousing 10. When thestorage hatch 20 is in the open position (FIG. 2A ) cuff retainers 55(a), 55(b) having retainer strap slits 56(a), 56(b) positioned on opposite sides of theendotracheal tube 45, may be made available to assist the user in removing theendotracheal tube 45 from thetube cavity 50. When thestorage hatch 20 is in the closed position (FIG. 2B ) the cuff retainers 55(a), 55(b) extend outside of thehousing 10. - As shown further in
FIGS. 14A-14D , other features of thedevice 500 may include a plurality of detents 85(a)-(c) positioned at prescribed intervals, scalpel distance demarcations 90(a)-(c) (indicating distances of 5 mm, 10 mm, and 15 mm),pushbutton housing 505. - Recessed
areas 535 may be provided on each side of thehousing 505 for grip and hook finger tab compression of each of thetissue spreader legs leg FIG. 14B ). In this regard, anLED lens 540 may be provided having an integrally molded locating support boss 545 for rotating the depth guard/“hook”/tissue spreader 530 and further includesdetents 550 for identifying the plurality of angle openings for eachleg -
FIGS. 15A-15F show a compact, hand-held, ergonomically designed, stand-alone device 600 having a combination tracheal “hook” 605 and tissue-spreader/dilator 610 integrally formed therein. Thecombination tool 600 is of a generally durable, sterilizable, single-piece injection molded construction. As shown in the figures, thecombination device 600 includes anelongated body 615 having a tracheal “hook” 605 at one end and a curved “trosseau”style dilator 610 with a bifurcated “slide-ratchet”track 620 for opening and closing the dilator or tissue spreader tips ortines device 600. - In this regard, the “slide-ratchet”
track 620 may further include anactuator handle 630, a “scissors” shaped gripping means in one embodiment, having an attachedpost 635 for operable engagement with thetrack 620 to incrementally open and close thedilator 610. Thepost 635 provides for ratcheted/notched engagement of the actuator handle 630 with corresponding detents ornotches 640 positioned alongopposite sides bifurcated track 620. In this regard, as thehandle 630 is moved along thetrack 620 in one direction thedilator 610 is incrementally opened. When thehandle 630 is moved along thetrack 620 in the opposite direction thedilator 610 is incrementally closed. - As indicated in the figures, in one embodiment, the overall length of the
device 600 is approximately 5.5 inches (FIG. 15A ), while the closed or “neutral” static state width of thedilator 610 is approximately 0.130 inches (FIG. 15B ) and the maximum opened state of the dilator is approximately 0.625 inches (FIG. 15C ). Persons of ordinary skill in the art will understand that these dimensions are for illustrative purposes and that these and other dimensions shown in the figures may be varied depending on a various factors. -
FIGS. 16-19 show another embodiment of a durable, compact, lightweight, ergonomic hand-held device having universal and common components and methodology of execution for use in, among other things, one-hand operation in providing an opening into the body such as in establishing an airway in medical procedures. - The
device 700 includes ahousing 705 having first andsecond sidewalls device 700. - The
device 700 further includes afirst slider unit 710 for extending and retracting ascalpel 711, and asecond slider unit 720 for extending and retracting abifurcated tissue spreader 721. In this regard, thescalpel 711 is operably connected to itsrespective slider unit 710 by well-known means such as those methods use to retain the blade of a box cutter. In this regard, the scalpel may include an orifice or cutout (not shown) for mating with a correspondingly shapedprotrusion 719 formed in thefirst slider unit 710. - The
bifurcated tissue spreader 721 includes a firstelongated arm 722 and a secondelongated arm 723 each having ahollow barrel 722 a, 723 a formed at one end of the respective first and secondelongated arms hollow barrels 722 a, 723 a are position atop each other and between upper and lower portions of a “C”section 724 formed in thesecond slider unit 720 where a retainingpin 726 positioned through the hollow barrels 72 a, 723 a holds the first and secondelongated arms tissue spreader 721 in place in thesecond slider unit 720. - In one embodiment, the first and second
elongated arms tissue spreader 721 may each include a “hooked”distal portion - In a retracted position the
scalpel 711 andtissue spreader 721 are disposed or stored safely and conveniently within thehousing 705. Thefirst slider unit 710 and thesecond slider unit 720 are positioned within aslider track 730 formed in the first andsecond sidewalls slider track 730 permits thescalpel 711 andtissue spreader 721 to be extended away from thehousing 705 and retracted toward thehousing 705. In other words, in one embodiment, thedevice 700 described herein provides for retractable deployment, i.e., extension and retraction of ascalpel 711 and atissue spreader 721 along acommon slider track 730. - In one embodiment, the first or
scalpel slider unit 710 is positioned forward of the second or tissuespreader slider unit 720 within theslider track 730 for retractable deployment from the same side/end (first end 707 a) of thedevice 700. A spring orsimilar tensioning device 725 is operably connected to thefirst slider unit 710 along ahooked protrusion 727 and to one of the first orsecond sidewalls first slider switch 710 while in the extended position. In this regard, as explained below, in one embodiment thefirst slider unit 710 is moved along theslider track 730 to extend and lock thescalpel 711 into position from thehousing 705. Thesecond slider unit 720 is then moved along theslider track 730 in the same direction and as thefirst slider switch 710 to auto-retract thescalpel 711 while simultaneously extending and spreading thebifurcated tissue spreader 721. - In this regard, the term “auto-retract” is understood to mean that a single action (movement of the
second slider unit 720 and its corresponding tissue spreader 721) causes a second action (retraction of thefirst slider unit 710 and its associated scalpel 711) to occur. (In actuality, as explained below, movement of thesecond slider unit 720 further causes a third action, that is, the spreading apart of thearms tissue spreader 721 to occur.) Accordingly, under one set of conditions, the structural configuration and positioning of thefirst slider unit 710 and thesecond slider unit 720 on thesame slider track 730 results in a “cause and affect” relationship between the twounits second slider unit 720 causes thefirst slider unit 710 to retract as a result of the attached spring (725) returning to its normal “relaxed” state. - As further shown in
FIGS. 18 and 19 , thehousing 705 also provides for switch and/orpushbutton light spectrum LEDs housing 705. Lithium ion batterie(s) 728 are positioned within thehousing 705 to provide power to theLEDs pushbuttons LEDs ribbon 737, as shown inFIG. 17 . - “Gripper nubs” (raised bumps) 745, shown in
FIG. 16 , may be molded into thehousing 705 or formed from rubber and applied to thehousing 705 to provide a textured surface to assist the user in holding, gripping, or otherwise maneuvering thedevice 700. - As shown in
FIG. 18 , thedevice 700 may further include anelongated carriage 750 formed from the joined together sidewalls 706 a, 706 b of thedevice 700 and a protrudingclip 755 each extending from asecond end 707 b opposite thefirst end 707 a of thedevice 700. In this regard, the protrudingclip 755 is positioned in close proximity to the underside of thesidewalls clip 755 and the underside of thesidewalls - The
elongated carriage 750 having spaced apart sides 751 a, 751 b and the protrudingclip 755 form or define an open-well orcompartment 765 for retaining an airway tube 770 (FIG. 16 ) and sterile gaze (not shown). In this regard, thecarriage 750 further includes a curveddistal portion 752 formed by the spaced apart sides 751 a, 751 b. Thedistal portion 752 of thecarriage 750 is shaped to correspond to the shape of theairway tube 770 retained therebetween and may further be configured to allow thedistal portion 752, i.e., spaced apart sides 751 a, 751 b to flex apart and return to their original position due to material memory to assist in holding one end ofairway tube 770 in place. A retaining or mountingstem 775 having an O-ring 780 positioned around the mountingstem 775 may further be including and positioned along anupper area 776 of thedevice 700 to assist in holding the opposite end of theairway tube 700 in place. - As indicated above and shown in
FIGS. 20A and 20B , thedevice 700 includes afirst slider unit 710 for extending and retracting ascalpel 711, and asecond slider unit 720 for extending and retracting abifurcated tissue spreader 721 along acommon slider track 730 formed between first andsecond sidewalls housing 705 to permit for retractable deployment and retraction of ascalpel 711 and atissue spreader 721 from the same side of thedevice 700. - As shown in
FIG. 20B , thefirst slider unit 710 having thescalpel 711 attached thereto is moved in a forward direction along theslider track 730 to extend thescalpel 711 from thehousing 705. In this regard, as best shown inFIG. 19 , thefirst slider unit 710 is movably retained within an elongatedtop rail 786 a and a correspondingelongated bottom rail 786 b of theslider track 730 formed in each of the first andsecond sidewalls first slider switch 710 along theslider track 730 until thefirst slider unit 710 is position between anupper forward portion 785 a of thetop rail 786 a and abottom forward portion 785 b of thebottom rail 786 b of each side theslider track 730, and a retaining nub 787 (FIG. 20B ) having a curved rearward surface formed on an outside surface of the each of thebottom rails 786 b formed inrespective sidewalls first slider unit 710 is retained in the forward position, despite tension from thespring 725 having been extended due to the forward movement of thefirst slider unit 710 along theslider track 730, by an “L” shaped retaininglip 788 located at one end of thefirst slider unit 710 being positioned against the retainingnubs 787. In this regard, the curved surface of the retainingnubs 787 permits the retaininglip 788 to be easily pushed passed the retainingnubs 787 when moved in a forward direction, but held relatively securely when attempting to move in the backward or rearward direction by a relatively flat surface back surface of the retaininglip 788. As such, thefirst slider unit 710 is retained in the forward position along theslider track 730 with thescalpel 711 extended. - In one embodiment, once the
first slider unit 710 is retained in the forward position thesecond slider unit 720 is moved in the forward direction to extend and expand the firstelongated arm 722 and the secondelongated arm 723 of thebifurcated tissue spreader 721, and to facilitate auto-retraction/release of thefirst slider unit 710. - In this regard, as shown in
FIGS. 19 , 20C and 20D, thesecond slider switch 720 is movably retained within the elongatedtop rail 786 a of theslider track 730 formed in each of the first andsecond sidewalls second slider unit 720 along theslider track 730. As indicated above, the firstelongated arm 722 and the secondelongated arm 723 of thebifurcated tissue spreader 721 are retained within the “C”section 724 formed in thesecond slider unit 720. The firstelongated arm 722 and the secondelongated arm 723 of thebifurcated tissue spreader 721 are further positioned such that one of theelongated arms housing 705 through afirst window 790 a formed in one of thesidewalls elongated arm housing 705 through asecond window 790 b opposite thefirst window 790 a to position each of theelongated arms device 700. - When moved in the forward direction along the slider track 730 a first
lateral sidewall portion 795 a formed between thetop rail 786 a and thebottom rail 786 b of theslider track 730 of thefirst sidewall 706 a, and a secondlateral sidewall portion 795 b formed between thetop rail 786 a and thebottom rail 786 b of theslider track 730 of thesecond sidewall 706 b force the firstelongated arm 722 and the secondelongated arm 723 apart (FIG. 20D ) as the first and secondlateral sidewall portions section 724 formed in the second slider unit 720 (connection point of the firstelongated arm 722 and the secondelongated arm 723 of the bifurcated tissue spreader 721). In one embodiment, the first and secondelongated arm - As the first and second
elongated arms lateral sidewall portions indented portion 796 a of the firstelongated arm 722 contacts afirst protrusion 797 a formed on the firstlateral sidewall portion 795 a. Likewise, a secondindented portion 796 b of the secondelongated arm 723 contacts a second protrusion (not shown) formed on the second lateral sidewall portion. Thebifurcated tissue spreader 721 is retained in this forward position by a firstelongated tension strip 798 a formed in thefirst sidewall 706 a and biased against the firstelongated arm 722, and a secondelongated tension strip 798 b formed in thesecond sidewall 706 b and biased against the secondelongated arm 723. - Movement of the
second slider unit 720 in the backward or rearward direction is accomplished by manually applying sufficient force to thesecond slider unit 720 in the backward direction to overcome the bias force applied by the first and second elongated tension strips 798 a, 798 b. - As indicated above, forward movement of the
second slider unit 720 facilitates auto-retraction of thefirst slider unit 710. In this regard, when thefirst slider unit 710 is retained in the forward position along theslider track 730 with thescalpel 711 extended and thesecond slider unit 720 is move in the forward direction, a curved shapedlower segment 799 of the “C”section 724 of thesecond slider unit 720 contacts and forces the retaininglip 788 of thefirst slider unit 710 to disengage from the retainingnubs 787 as thesecond slider unit 720 moves past the retaininglip 788 forcing the retaininglip 788 downward to permit thespring 725 to move thefirst slider unit 710 back to its original position within thehousing 705 with thescalpel 711 safely retracted (FIG. 20D ). - Forward and backward directional movement of the
second slider unit 720 may be accomplished independent of thefirst slider unit 710 and may be accomplished regardless of the position of thefirst slider unit 710 along theslider track 730. - Although methods are described and illustrated herein with steps occurring in a certain order, the specific order of the steps, or any continuation or interruption between steps, is not required.
- The apparatus and methods have been described with some particularity, but the specific designs, constructions and steps disclosed are not to be taken as delimiting. Obvious modifications will make themselves apparent to those of ordinary skill in the art, all of which will not depart from the essence and spirit of the subject matter described herein and all such changes and modifications are intended to be encompassed within the appended claims.
Claims (21)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/043,849 US8356598B2 (en) | 2007-04-17 | 2008-03-06 | Apparatus and related method for providing a passage into the body |
PCT/US2008/060247 WO2008130893A1 (en) | 2007-04-17 | 2008-04-14 | Apparatus and related method for providing a passage into the body |
EP08745781A EP2146618A4 (en) | 2007-04-17 | 2008-04-14 | Apparatus and related method for providing a passage into the body |
CA002682392A CA2682392A1 (en) | 2007-04-17 | 2008-04-14 | Apparatus and related method for providing a passage into the body |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US92385607P | 2007-04-17 | 2007-04-17 | |
US12/043,849 US8356598B2 (en) | 2007-04-17 | 2008-03-06 | Apparatus and related method for providing a passage into the body |
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US20080257359A1 true US20080257359A1 (en) | 2008-10-23 |
US8356598B2 US8356598B2 (en) | 2013-01-22 |
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US12/043,849 Active 2031-11-23 US8356598B2 (en) | 2007-04-17 | 2008-03-06 | Apparatus and related method for providing a passage into the body |
Country Status (4)
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US (1) | US8356598B2 (en) |
EP (1) | EP2146618A4 (en) |
CA (1) | CA2682392A1 (en) |
WO (1) | WO2008130893A1 (en) |
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US20100089405A1 (en) * | 2008-04-04 | 2010-04-15 | Tactical Medical Solutions, Inc. | Combination tracheal hook and surgical blade |
US20120204867A1 (en) * | 2009-10-15 | 2012-08-16 | Airway Cam Technologies, Inc. | Introducer for Surgical Airway Catheters |
US20120298102A1 (en) * | 2009-10-15 | 2012-11-29 | Airway Cam Technologies, Inc. | Introducer for Surgical Airway Catheters |
WO2013172998A2 (en) * | 2012-05-01 | 2013-11-21 | Huddleston Herbert D | Method and apparatus for minimally invasive skin and soft-tissue incisions |
EP2737862A1 (en) * | 2012-11-28 | 2014-06-04 | Richard M. Levitan | Surgical device for cricothyrotomy and the like |
US9167959B1 (en) * | 2010-03-26 | 2015-10-27 | Optech Ventures, Llc | Illumination for enhanced contrast in debridement apparatus and method |
US9393374B2 (en) | 2013-03-25 | 2016-07-19 | Richard M. Levitan | Introducer for surgical airway catheters |
US20170326318A1 (en) * | 2016-05-13 | 2017-11-16 | Richard Vanner | Cricothyrotomy introducer tool |
US11517349B2 (en) | 2019-09-27 | 2022-12-06 | Bard Access Systems, Inc. | Autovance feature of an intraosseous device |
US11633214B2 (en) | 2019-09-27 | 2023-04-25 | Bard Access Systems, Inc. | Various operating mechanisms for intraosseous access medical devices and methods thereof |
US11759235B2 (en) | 2019-09-27 | 2023-09-19 | Bard Access Systems, Inc. | Constant-torque intraosseous access devices and methods thereof |
US11883071B2 (en) | 2016-10-27 | 2024-01-30 | C. R. Bard, Inc. | Intraosseous access device |
US11896264B2 (en) | 2020-04-21 | 2024-02-13 | Bard Access Systems, Inc. | Reusable push-activated intraosseous access device |
US11925361B2 (en) | 2021-02-08 | 2024-03-12 | Bard Access Systems, Inc. | Intraosseous modular power |
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US9555206B1 (en) * | 2013-05-22 | 2017-01-31 | Mark Edward Tellam | Dilator device |
EP3096825B1 (en) * | 2014-01-22 | 2019-05-15 | University of Maryland, Baltimore | System for emergency apneic oxygenation |
US10524813B2 (en) | 2015-04-19 | 2020-01-07 | Bam Medical Ltd. | Frenulum spreader |
USD822207S1 (en) | 2017-03-03 | 2018-07-03 | Bam Medical Ltd. | Frenulum exercising tool |
EP3634557A4 (en) * | 2017-06-04 | 2021-03-10 | Unity Health Toronto | Tracheotomy device and method |
US11752289B2 (en) * | 2018-12-07 | 2023-09-12 | University Of Maryland, Baltimore | System and method for automatic emergency airway detection |
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Also Published As
Publication number | Publication date |
---|---|
WO2008130893A1 (en) | 2008-10-30 |
US8356598B2 (en) | 2013-01-22 |
EP2146618A1 (en) | 2010-01-27 |
CA2682392A1 (en) | 2008-10-30 |
EP2146618A4 (en) | 2011-09-07 |
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